"Mekewei" microporous membrane oxygenator with venous hard shell blood storage tank
Taiwan·Risk Class 2·Maquet Cardiopulmonary AG; MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti·Registered Dec 17, 2010 – Dec 17, 2025Expired- Analysis ID
- 7424074b9c4113c52365aead68cf88cc
- Customs Code
- DHA00602185903
- Manufacturer Country
- Türkiye;;Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4400 心肺血管繞道術血液儲存器;; E.4350 心肺血管繞道術和氧器
- Import Information
- import
- Registration Date
- Dec 17, 2010
- Expiry Date
- Dec 17, 2025
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Access comprehensive regulatory information for "Mekewei" microporous membrane oxygenator with venous hard shell blood storage tank in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7424074b9c4113c52365aead68cf88cc and manufactured by Maquet Cardiopulmonary AG; MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti;; Maquet Cardiopulmonary GmbH, Maquet Cardiopulmonary AG; MAQUET Cardiopulmonary Medikal Teknik San. Twitch. Ltd. Sti, and 3 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.